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Journal articles on the topic 'Electrostatic Assembly'

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Author: Grafiati

Published: 7 September 2023

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1

Martin, Lisal, Sindelka Karel, Sueha Lucie, Limpouchova Zuzana, and Prochazka Karel. "Dissipative Particle Dynamics Simulations of Polyelectrolyte Self-Assemblies. Methods with Explicit Electrostatics1, "Высокомолекулярные соединения. Серия С"." Высокомолекулярные соединения С, no. 1 (2017): 82–107. http://dx.doi.org/10.7868/s2308114717010101.

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Abstract - This feature article is addressed to a broad community of polymer scientists, both theoreticians and experimentalists. We present several examples of our dissipative particle dynamics (DPD) simulations of self- and co-assembling polyelectrolyte systems to illustrate the power of DPD. In the first part, we briefly outline basic principles of DPD. Special emphasis is placed on the incorporation of explicit electrostatic forces into DPD, on their calibration with respect to the soft repulsion forces and on the use of DPD for studying the self-assembly of electrically charged polymer systems. At present, the method with explicit electrostatics is being used in a number of studies of the behavior of single polyelectrolyte chains, their interaction with other components of the system, etc. However, in DPD studies of self-assembly, which require high numbers of chains, only a few research groups use explicit electrostatics. Most studies of polyelectrolyte self-assembly are based on the “implicit solvent ionic strength” approach, which completely ignores the long-range character of electrostatic interactions, because their evaluation complicates and considerably slows down the DPD simulation runs. We aim at the analysis of the impact of explicit electrostatics on simulation results.

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2

Xian, Yuejiao, Chitra B. Karki, Sebastian Miki Silva, Lin Li, and Chuan Xiao. "The Roles of Electrostatic Interactions in Capsid Assembly Mechanisms of Giant Viruses." International Journal of Molecular Sciences 20, no. 8 (April 16, 2019): 1876. http://dx.doi.org/10.3390/ijms20081876.

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In the last three decades, many giant DNA viruses have been discovered. Giant viruses present a unique and essential research frontier for studies of self-assembly and regulation of supramolecular assemblies. The question on how these giant DNA viruses assemble thousands of proteins so accurately to form their protein shells, the capsids, remains largely unanswered. Revealing the mechanisms of giant virus assembly will help to discover the mysteries of many self-assembly biology problems. Paramecium bursaria Chlorella virus-1 (PBCV-1) is one of the most intensively studied giant viruses. Here, we implemented a multi-scale approach to investigate the interactions among PBCV-1 capsid building units called capsomers. Three binding modes with different strengths are found between capsomers around the relatively flat area of the virion surface at the icosahedral 2-fold axis. Furthermore, a capsomer structure manipulation package is developed to simulate the capsid assembly process. Using these tools, binding forces among capsomers were investigated and binding funnels were observed that were consistent with the final assembled capsid. In addition, total binding free energies of each binding mode were calculated. The results helped to explain previous experimental observations. Results and tools generated in this work established an initial computational approach to answer current unresolved questions regarding giant virus assembly mechanisms. Results will pave the way for studying more complicated process in other biomolecular structures.

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3

Zhang, Peng, Fenghuan Wang, Yuxuan Wang, Shuangyang Li, and Sai Wen. "Self-Assembling Behavior of pH-Responsive Peptide A6K without End-Capping." Molecules 25, no. 9 (April 26, 2020): 2017. http://dx.doi.org/10.3390/molecules25092017.

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A short self-assembly peptide A6K (H2N−AAAAAAK−OH) with unmodified N− and C−terminus was designed, and the charge distribution model of this short peptide at different pH was established by computer simulation. The pH of the solution was adjusted according to the model and the corresponding self-assembled structure was observed using a transmission electron microscope (TEM). As the pH changes, the peptide will assemble into blocks or nanoribbons, which indicates that the A6K peptide is a pH-responsive peptide. Circular dichroism (CD) and molecular dynamics (MD) simulation showed that the block structure was formed by random coils, while the increase in β-turn content contributes to the formation of intact nanoribbons. A reasonable explanation of the self-assembling structure was made according to the electrostatic distribution model and the effect of electrostatic interaction on self-assembly was investigated. This study laid the foundation for further design of nanomaterials based on pH-responsive peptides.

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4

Tien, Joe, Andreas Terfort, and George M. Whitesides. "Microfabrication through Electrostatic Self-Assembly." Langmuir 13, no. 20 (October 1997): 5349–55. http://dx.doi.org/10.1021/la970454i.

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5

Ma, Yujie, Mark A. Hempenius, and G. Julius Vancso. "Electrostatic Assembly with Poly(ferrocenylsilanes)." Journal of Inorganic and Organometallic Polymers and Materials 17, no. 1 (February 16, 2007): 3–18. http://dx.doi.org/10.1007/s10904-006-9081-4.

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6

Kutz, A., G. Mariani, R. Schweins, C. Streb, and F. Gröhn. "Self-assembled polyoxometalate–dendrimer structures for selective photocatalysis." Nanoscale 10, no. 3 (2018): 914–20. http://dx.doi.org/10.1039/c7nr07097g.

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7

Han, Songling, Huijie An, Hui Tao, Lanlan Li, Yuantong Qi, Yongchang Ma, Xiaohui Li, Ruibing Wang, and Jianxiang Zhang. "Advanced emulsions via noncovalent interaction-mediated interfacial self-assembly." Chemical Communications 54, no. 25 (2018): 3174–77. http://dx.doi.org/10.1039/c8cc00016f.

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The traditional emulsification theory is enriched by a self-assembly approach, in which hydrophilic copolymers with one block exhibiting electrostatic or hydrogen-bonding forces with the oil phase self-assemble at the oil–water interface, thereby reducing interfacial tension and forming emulsions.

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8

Konopelnyk, O. I. "Electrostatic layer-by-layer assembly of poly-3,4-ethylene dioxythiophene functional nanofilms." Functional materials 20, no. 2 (June 25, 2013): 248–52. http://dx.doi.org/10.15407/fm20.02.248.

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9

Svensson, Fredric G., Gulaim A. Seisenbaeva, Nicholas A. Kotov, and Vadim G. Kessler. "Self-Assembly of Asymmetrically Functionalized Titania Nanoparticles into Nanoshells." Materials 13, no. 21 (October 29, 2020): 4856. http://dx.doi.org/10.3390/ma13214856.

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Titania (anatase) nanoparticles were anisotropically functionalized in water-toluene Pickering emulsions to self-assemble into nanoshells with diameters from 500 nm to 3 μm as candidates for encapsulation of drugs and other compounds. The water-phase contained a hydrophilic ligand, glucose-6-phosphate, while the toluene-phase contained a hydrophobic ligand, n-dodecylphosphonic acid. The addition of a dilute sodium alginate suspension that provided electrostatic charge was essential for the self-limited assembly of the nanoshells. The self-assembled spheres were characterized by scanning electron microscopy, elemental mapping, and atomic force microscopy. Drug release studies using tetracycline suggest a rapid release dominated by surface desorption.

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10

Oertel, Catherine. "Photodetectors Fabricated Using Electrostatic Self-Assembly." MRS Bulletin 29, no. 3 (March 2004): 136–37. http://dx.doi.org/10.1557/mrs2004.43.

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11

Sastry, Murali, Mala Rao, and Krishna N. Ganesh. "Electrostatic Assembly of Nanoparticles and Biomacromolecules." Accounts of Chemical Research 35, no. 10 (October 2002): 847–55. http://dx.doi.org/10.1021/ar010094x.

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12

Hu, Tao, Rui Zhang, and B. I. Shklovskii. "Electrostatic theory of viral self-assembly." Physica A: Statistical Mechanics and its Applications 387, no. 12 (May 2008): 3059–64. http://dx.doi.org/10.1016/j.physa.2008.01.010.

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13

Hees, Jakob, Armin Kriele, and Oliver A. Williams. "Electrostatic self-assembly of diamond nanoparticles." Chemical Physics Letters 509, no. 1-3 (June 2011): 12–15. http://dx.doi.org/10.1016/j.cplett.2011.04.083.

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14

Mici, Joni, Jang Won Ko, Jared West, Jeffrey Jaquith, and Hod Lipson. "Parallel electrostatic grippers for layered assembly." Additive Manufacturing 27 (May 2019): 451–60. http://dx.doi.org/10.1016/j.addma.2019.03.032.

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15

Willerich, Immanuel, and Franziska Gröhn. "Photoswitchable Nanoassemblies by Electrostatic Self-Assembly." Angewandte Chemie International Edition 49, no. 44 (August 26, 2010): 8104–8. http://dx.doi.org/10.1002/anie.201003271.

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16

Muto, Hiroyuki, Atsushi Yokoi, and Wai Kian Tan. "Electrostatic Assembly Technique for Novel Composites Fabrication." Journal of Composites Science 4, no. 4 (October 20, 2020): 155. http://dx.doi.org/10.3390/jcs4040155.

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Electrostatic assembly is one of the bottom–up approaches used for multiscale composite fabrication. Since its discovery, this method has been actively used in molecular bioscience as well as materials design and fabrication for various applications. Despite the recent advances and controlled assembly reported using electrostatic interaction, the method still possesses vast potentials for various materials design and fabrication. This review article is a timely revisit of the electrostatic assembly method with a brief introduction of the method followed by surveys of recent advances and applications of the composites fabricated. Emphasis is also given to the significant potential of this method for advanced materials and composite fabrication in line with sustainable development goals. Prospective outlook and future developments for micro-/nanocomposite materials fabrication for emerging applications such as energy-related fields and additive manufacturing are also mentioned.

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17

Sastry, Murali. "Assembling nanoparticles and biomacromolecules using electrostatic interactions." Pure and Applied Chemistry 74, no. 9 (January 1, 2002): 1621–30. http://dx.doi.org/10.1351/pac200274091621.

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Nanotechnology is witnessing impressive advances on many different fronts. One of the key areas with important commercial implications concerns the assembly of nanoparticles to form thin films and superstructures by what is commonly known as the "bottom-up" approach. This paper covers some of the more recent developments in this fascinating field with particular emphasis on the work from the author's laboratory on assembly of nanoparticles using electrostatic interactions. The use of electrostatic interactions enables extension of the assembly protocols to the immobilization of biomacromolecules such as proteins/enzymes and DNA with exciting application potential.

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18

Mao, Shun, Ganhua Lu, Kehan Yu, and Junhong Chen. "Protein Viability on Au Nanoparticles during an Electrospray and Electrostatic-Force-Directed Assembly Process." Journal of Nanomaterials 2010 (2010): 1–6. http://dx.doi.org/10.1155/2010/196393.

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We study the protein viability on Au nanoparticles during an electrospray and electrostatic-force-directed assembly process, through which Au nanoparticle-antibody conjugates are assembled onto the surface of carbon nanotubes (CNTs) to fabricate carbon nanotube field-effect transistor (CNTFET) biosensors. Enzyme-linked immunosorbent assay (ELISA) and field-effect transistor (FET) measurements have been used to investigate the antibody activity after the nanoparticle assembly. Upon the introduction of matching antigens, the colored reaction from the ELISA and the change in the electrical characteristic of the CNTFET device confirm that the antibody activity is preserved during the assembly process.

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19

Wang, Wei-Chih, Yen-Tse Cheng, and Benjamin Estroff. "Electrostatic Self-Assembly of Composite Nanofiber Yarn." Polymers 13, no. 1 (December 22, 2020): 12. http://dx.doi.org/10.3390/polym13010012.

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Electrospinning polymer fibers is a well-understood process primarily resulting in random mats or single strands. More recent systems and methods have produced nanofiber yarns (NFY) for ease of use in textiles. This paper presents a method of NFY manufacture using a simplified dry electrospinning system to produce self-assembling functional NFY capable of conducting electrical charge. The polymer is a mixture of cellulose nanocrystals (CNC), polyvinyl acrylate (PVA) and poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS). When treated with ethylene glycol (EG) to enhance conductivity, fibers touching the collector plate align to the applied electrostatic field and grow by twisting additional nanofiber polymers injected by the jet into the NFY bundle. The longer the electrospinning continues, the longer and more uniformly twisted the NFY becomes. This process has the added benefit of reducing the electric field required for NFY production from >2.43 kV cm−1 to 1.875 kV cm−1.

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20

Uğur, Şule S., and Merih Sarıışık. "Electrostatic self-assembly dyeing of cotton fabrics." Coloration Technology 127, no. 6 (October 27, 2011): 372–75. http://dx.doi.org/10.1111/j.1478-4408.2011.00328.x.

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21

Kostiainen, Mauri A., Panu Hiekkataipale, Jose Á. de la Torre, Roeland J. M. Nolte, and Jeroen J. L. M. Cornelissen. "Electrostatic self-assembly of virus–polymer complexes." J. Mater. Chem. 21, no. 7 (2011): 2112–17. http://dx.doi.org/10.1039/c0jm02592e.

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22

TEZUKA, Yasuyuki. "Topological Polymer Chemistry by Electrostatic Self-Assembly." Kobunshi 53, no. 8 (2004): 575–78. http://dx.doi.org/10.1295/kobunshi.53.575.

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23

Liang, Hongjun, Gregg Whited, Chi Nguyen, Adam Okerlund, and Galen D. Stucky. "Inherently Tunable Electrostatic Assembly of Membrane Proteins." Nano Letters 8, no. 1 (January 2008): 333–39. http://dx.doi.org/10.1021/nl0729173.

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24

Jing, Yang, Wang Yan, and Xu Xiaowen. "Preparation of Mesoporous SnO2by Electrostatic Self-Assembly." Journal of Chemistry 2014 (2014): 1–7. http://dx.doi.org/10.1155/2014/713573.

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We report a simple and scalable strategy to synthesize mesoporous SnO2with tin dioxide nanoparticles of 5-6 nm crystalline walls and 3-4 nm pore diameter with the assistance ofMo7O246-as templating agent at room temperature. The samples were characterized by XRD, TEM, UV-DRS, XPS, and BET. The product has a moderately high surface area of 132 m2 g−1and a narrow mesoporous structure with an average pore diameter of 3.5 nm. The photocatalytic activities of the mesoporous SnO2were evaluated by the degradation of methyl orange (MO) in aqueous solution under UV light irradiation.

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25

Ardanuç, S. M., and A. Lal. "Ultrasound enhanced electrostatic batch assembly for MEMS." Sensors and Actuators A: Physical 197 (August 2013): 136–49. http://dx.doi.org/10.1016/j.sna.2013.03.017.

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26

McDermott, Joseph J., Neetu Chaturvedi, and Darrell Velegol. "Functional colloidal trimers by quenched electrostatic assembly." Physical Chemistry Chemical Physics 12, no. 38 (2010): 11930. http://dx.doi.org/10.1039/c0cp00254b.

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27

Baur, J. W., M. F. Durstock, B. E. Taylor, R. J. Spry, S. Reulbach, and L. Y. Chiang. "Photovoltaic interface modification via electrostatic self-assembly." Synthetic Metals 121, no. 1-3 (March 2001): 1547–48. http://dx.doi.org/10.1016/s0379-6779(00)01231-5.

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28

Mendes, Ana C., Timm Strohmenger, Francisco Goycoolea, and Ioannis S. Chronakis. "Electrostatic self-assembly of polysaccharides into nanofibers." Colloids and Surfaces A: Physicochemical and Engineering Aspects 531 (October 2017): 182–88. http://dx.doi.org/10.1016/j.colsurfa.2017.07.044.

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29

Tezuka, Yasuyuki. "Topological polymer chemistry by electrostatic self-assembly." Journal of Polymer Science Part A: Polymer Chemistry 41, no. 19 (August 27, 2003): 2905–17. http://dx.doi.org/10.1002/pola.10893.

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30

Maas, Michael, Carolina C. Silvério, Jens Laube, and Kurosch Rezwan. "Electrostatic assembly of zwitterionic and amphiphilic supraparticles." Journal of Colloid and Interface Science 501 (September 2017): 256–66. http://dx.doi.org/10.1016/j.jcis.2017.04.076.

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31

Jang, Woo-Sik, Tomonori Saito, Michael A. Hickner, and Jodie L. Lutkenhaus. "Electrostatic Assembly of Poly(ethylene glycol) Nanotubes." Macromolecular Rapid Communications 31, no. 8 (March 1, 2010): 745–51. http://dx.doi.org/10.1002/marc.200900807.

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32

Detig, Robert H. "Electrostatic Self Assembly Of Carbon Nano-Tubes." NIP & Digital Fabrication Conference 24, no. 1 (January 1, 2008): 895–96. http://dx.doi.org/10.2352/issn.2169-4451.2008.24.1.art00111_2.

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33

Button, Julie M., and Suchetana Mukhopadhyay. "Removing the Polyanionic Cargo Requirement for Assembly of Alphavirus Core-Like Particles to Make an Empty Alphavirus Core." Viruses 12, no. 8 (August 3, 2020): 846. http://dx.doi.org/10.3390/v12080846.

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The assembly of alphavirus nucleocapsid cores requires electrostatic interactions between the positively charged N-terminus of the capsid protein (CP) and the encapsidated polyanionic cargo. This system differs from many other viruses that can self-assemble particles in the absence of cargo, or form “empty” particles. We hypothesized that the introduction of a mutant, anionic CP could replace the need for charged cargo during assembly. In this work, we produced a CP mutant, Minus 38 (M38), where all N-terminal charged residues are negatively-charged. When wild-type (WT) and M38 CPs were mixed, they assembled into core-like particles (CLPs). These “empty” particles were of similar size and morphology to WT CLPs assembled with DNA cargo, but did not contain nucleic acid. When DNA cargo was added to the assembly mixture, the amount of M38 CP that was assembled into CLPs decreased, but was not fully excluded from the CLPs, suggesting that M38 competes with DNA to interact with WT CPs. The composition of CLPs can be tuned by altering the order of addition of M38 CP, WT CP, and DNA cargo. The ability to produce alphavirus CLPs that contain a range of amounts of encapsidated cargo, including none, introduces a new platform for packaging cargo for delivery or imaging purposes.

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34

Mali, Kunal S., and Steven De Feyter. "Principles of molecular assemblies leading to molecular nanostructures." Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 371, no. 2000 (October 13, 2013): 20120304. http://dx.doi.org/10.1098/rsta.2012.0304.

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Self-assembled physisorbed monolayers consist of regular two-dimensional arrays of molecules. Two-dimensional self-assembly of organic and metal–organic building blocks is a widely used strategy for nanoscale functionalization of surfaces. These supramolecular nanostructures are typically sustained by weak non-covalent forces such as van der Waals, electrostatic, metal–ligand, dipole–dipole and hydrogen bonding interactions. A wide variety of structurally very diverse monolayers have been fabricated under ambient conditions at the liquid–solid and air–solid interface or under ultra-high-vacuum (UHV) conditions at the UHV–solid interface. The outcome of the molecular self-assembly process depends on a variety of factors such as the nature of functional groups present on assembling molecules, the type of solvent, the temperature at which the molecules assemble and the concentration of the building blocks. The objective of this review is to provide a brief account of the progress in understanding various parameters affecting two-dimensional molecular self-assembly through illustration of some key examples from contemporary literature.

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35

Deng, Yonghong, Yuan Wu, Yong Qian, Xinping Ouyang, Dongjie Yang, and Xueqing Qiu. "Adsorption and desorption behaviors of lignosulfonate during the self-assembly of multilayers." BioResources 5, no. 2 (April 18, 2010): 1178–96. http://dx.doi.org/10.15376/biores.5.2.1178-1196.

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Self-assembled multilayers were fabricated from lignosulfonate (LS) and poly(diallyldimethylammonium chloride) (PDAC), and the adsorption and desorption behaviors of LS on the LS/PDAC multilayers under different pH conditions were intensively investigated. Results showed that the adsorption and desorption behaviors were controlled by electrostatic attraction, hydrophobic interaction, and changes in the microstructure, which depended on solution pH. Lignosulfonates exist as colloids in solutions at low pH because of a hydrophobic interactions, and the LS colloids adsorbed on the PDAC layer because of electrostatic attraction. LS colloids started to disassociate at pH 3.5, resulting in an abrupt rise of the adsorption rate, a sharp decrease of the adsorbed amount, and a steep reduction in the surface roughness. Desorption behaviors of LS multilayers were related to the pH values of both LS dipping solution for self-assembly and the immersing solution for post-preparation treatment. Desorption of LS could be induced by a weakening of electrostatic attraction or hydrophobic interaction. A significant desorption occurred only when LS colloids dissociated in the multilayers. LS colloids were harder to dissociate in the multilayers than in the solutions because of electrostatic attraction between LS and PDAC.

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36

Pei, Xiao-Zhe, Shou-Qing Liu, and Wei-Hui Sun. "Cetyltrimethylammonium micelles enhance the sensitivity of ssDNA-based electrochemical sensor for the determination of pyridoxol." Anal. Methods 6, no. 14 (2014): 5127–32. http://dx.doi.org/10.1039/c4ay00847b.

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CTAB surfactant was assembled on ssDNA film electrode by electrostatic attraction between CTAB and ssDNA. The self-assembly of CTAB on ssDNA formed the micellar bilayer. Pyridoxol anions adsorbed on the micellar bilayer resulted in a markedly enhanced sensitivity. Practical applicability can be realized by the direct assay of pharmaceutical samples.

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37

Shen, Liangliang, Yahui Li, Qunzan Lu, Xiaoliang Qi, Xuan Wu, Zaigang Zhou, and Jianliang Shen. "Directed arrangement of siRNA via polymerization-induced electrostatic self-assembly." Chemical Communications 56, no. 16 (2020): 2411–14. http://dx.doi.org/10.1039/c9cc08858j.

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38

Velleman, L., L. Scarabelli, D. Sikdar, A. A. Kornyshev, L. M. Liz-Marzán, and J. B. Edel. "Monitoring plasmon coupling and SERS enhancement through in situ nanoparticle spacing modulation." Faraday Discussions 205 (2017): 67–83. http://dx.doi.org/10.1039/c7fd00162b.

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Self-assembled nanoparticle (NP) arrays at liquid interfaces provide a unique optical response which has opened the door to new tuneable metamaterials for sensing and optical applications. NPs can spontaneously assemble at a liquid–liquid interface, forming an ordered, self-healing, low-defect 2D film. The close proximity of the NPs at the interface results in collective plasmonic modes with a spectral response dependent on the distance between the NPs and induces large field enhancements within the gaps. In this study, we assembled spherical and rod-shaped gold NPs with the aim of improving our understanding of NP assembly processes at liquid interfaces, working towards finely controlling their structure and producing tailored optical and enhanced Raman signals. We systematically tuned the assembly and spacing between NPs through increasing or decreasing the degree of electrostatic screening with the addition of electrolyte or pH adjustment. The in situ modulation of the nanoparticle position on the same sample allowed us to monitor plasmon coupling and the resulting SERS enhancement processes in real time, with sub-nm precision.

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39

Lindgren, Eric B., Benjamin Stamm, Yvon Maday, Elena Besley, and A. J. Stace. "Dynamic simulations of many-body electrostatic self-assembly." Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 376, no. 2115 (February 5, 2018): 20170143. http://dx.doi.org/10.1098/rsta.2017.0143.

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Two experimental studies relating to electrostatic self-assembly have been the subject of dynamic computer simulations, where the consequences of changing the charge and the dielectric constant of the materials concerned have been explored. One series of calculations relates to experiments on the assembly of polymer particles that have been subjected to tribocharging and the simulations successfully reproduce many of the observed patterns of behaviour. A second study explores events observed following collisions between single particles and small clusters composed of charged particles derived from a metal oxide composite. As before, observations recorded during the course of the experiments are reproduced by the calculations. One study in particular reveals how particle polarizability can influence the assembly process. This article is part of the theme issue ‘Modern theoretical chemistry’.

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40

BHATIA, VASUDA, VIKESH GAUR, and VINOD K. JAIN. "NEW TECHNIQUE TO DEPOSIT THIN FILMS OF CARBON NANOTUBES BASED ON ELECTROSTATIC CHARGE DEPOSITION AND THEIR APPLICATION FOR ALCOHOL DETECTION." International Journal of Nanoscience 08, no. 04n05 (August 2009): 443–53. http://dx.doi.org/10.1142/s0219581x09006298.

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A new technique based on an electrostatic-force-directed-self-assembly was developed to fabricate thin films of multi-walled carbon nanotubes (MWCNTs) on thin dielectric wires. This technique was further developed to achieve functionalization of the nanotubes via acid-free dry route in a few seconds. The functionalization was confirmed by Fourier transform infrared and Raman spectroscopic measurements. The electrostatically self-assembled films provided significantly enhanced sensitivity for detection of alcohol vapors. Sensors were tested for response of alcohol concentrations as low as 200 ppm (parts per million) with a sensitivity of 4% and high repeatability. Recovery of sensors was observed to be within 200 s. Selectivity of the sensors for different organic vapors was defined based on the recovery time. Operation of sensors did not require high temperatures. It was realized that corona-based electrostatic self-assembly (CESA) pattering technique for batch fabrication of the sensors was fast, simple, low-cost, and required no specialized equipment.

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41

Lopez-Hernandez, Alan E., Yixin Xie, Wenhan Guo, and Lin Li. "The Electrostatic Features of Dengue Virus Capsid Assembly." Journal of Computational Biophysics and Chemistry 20, no. 02 (March 2021): 201–7. http://dx.doi.org/10.1142/s2737416520420089.

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Dengue virus causes serious diseases and deaths in the world. Understanding the fundamental mechanisms of dengue virus is highly demanded to develop treatments for dengue virus caused diseases. Here, we present a computational work which focused on the stability of dengue viral capsid. The interactions among E proteins on the dengue viral capsid were studied using several computational approaches. It was found that the electrostatic distribution on a single E protein monomer is highly inhomogeneous, which makes an E protein strongly binding with another E protein. This is the reason why all the E proteins form homodimers as the basic units on the whole dengue viral capsids. The pKa calculations of E proteins demonstrated that the folding energy of an E protein is low and stable in the range of pH 6–10, which is different from many other proteins that are stable at certain pH. The pH dependence of binding energy of E protein homodimer shows that the binding energy is low and independent from pH when the pH is also in the range of 6–10. This finding implies that the dengue virus can survive in a wide range of pH, which can explain why the dengue virus is so widely distributed in the world and spreads fast.

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42

Chang, Lan-Yun, Eiji Ōsawa, and Amanda S. Barnard. "Confirmation of the electrostatic self-assembly of nanodiamonds." Nanoscale 3, no. 3 (2011): 958. http://dx.doi.org/10.1039/c0nr00883d.

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43

Connolly, Audrey, and Etienne Gagnon. "Electrostatic interactions: From immune receptor assembly to signaling." Immunological Reviews 291, no. 1 (August 12, 2019): 26–43. http://dx.doi.org/10.1111/imr.12769.

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Xu, Longshan, Xiaohua Chen, Weiying Pan, Wenhua Li, Zhi Yang, and Yuxing Pu. "Electrostatic-assembly carbon nanotube-implanted copper composite spheres." Nanotechnology 18, no. 43 (October 4, 2007): 435607. http://dx.doi.org/10.1088/0957-4484/18/43/435607.

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Balach, Juan, Mariano M. Bruno, N. Gustavo Cotella, Diego F. Acevedo, and César A. Barbero. "Electrostatic self-assembly of hierarchical porous carbon microparticles." Journal of Power Sources 199 (February 2012): 386–94. http://dx.doi.org/10.1016/j.jpowsour.2011.10.029.

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Wu, Aiguo, Wenlong Cheng, Zhuang Li, Junguang Jiang, and Erkang Wang. "Electrostatic-assembly metallized nanoparticles network by DNA template." Talanta 68, no. 3 (January 15, 2006): 693–99. http://dx.doi.org/10.1016/j.talanta.2005.05.024.

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Hammond, Paula T. "Recent explorations in electrostatic multilayer thin film assembly." Current Opinion in Colloid & Interface Science 4, no. 6 (December 1999): 430–42. http://dx.doi.org/10.1016/s1359-0294(00)00022-4.

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Wang, Li, Gang Wei, Bin Qi, Hualan Zhou, Zhiguo Liu, Yonghai Song, Xiurong Yang, and Zhuang Li. "Electrostatic assembly of Cu2O nanoparticles on DNA templates." Applied Surface Science 252, no. 8 (February 2006): 2711–16. http://dx.doi.org/10.1016/j.apsusc.2005.03.212.

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Rha, Allisandra K., Dibyendu Das, Olga Taran, Yonggang Ke, Anil K. Mehta, and David G. Lynn. "Electrostatic Complementarity Drives Amyloid/Nucleic Acid Co‐Assembly." Angewandte Chemie International Edition 59, no. 1 (November 14, 2019): 358–63. http://dx.doi.org/10.1002/anie.201907661.

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Rha, Allisandra K., Dibyendu Das, Olga Taran, Yonggang Ke, Anil K. Mehta, and David G. Lynn. "Electrostatic Complementarity Drives Amyloid/Nucleic Acid Co‐Assembly." Angewandte Chemie 132, no. 1 (November 14, 2019): 366–71. http://dx.doi.org/10.1002/ange.201907661.

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